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Journal Abstract Search

256 related items for PubMed ID: 12116157

  • 1.
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  • 2. High-throughput single nucleotide polymorphism typing by fluorescent single-strand conformation polymorphism analysis with capillary electrophoresis.
    Doi K, Doi H, Noiri E, Nakao A, Fujita T, Tokunaga K.
    Electrophoresis; 2004 Mar; 25(6):833-8. PubMed ID: 15004843
    [Abstract] [Full Text] [Related]

  • 3. SNP genotyping by multiplexed solid-phase amplification and fluorescent minisequencing.
    Shapero MH, Leuther KK, Nguyen A, Scott M, Jones KW.
    Genome Res; 2001 Nov; 11(11):1926-34. PubMed ID: 11691857
    [Abstract] [Full Text] [Related]

  • 4. [A minisequencing technique for genotyping 12 Y-SNP and its genetic polymorphisms].
    Du H, Zhang L, Zhou B, Zhang HJ, Liang WB, Shen YH.
    Fa Yi Xue Za Zhi; 2006 Apr; 22(2):125-9. PubMed ID: 16850599
    [Abstract] [Full Text] [Related]

  • 5. Genotyping single-nucleotide polymorphisms by minisequencing using tag arrays.
    Lovmar L, Syvänen AC.
    Methods Mol Med; 2005 Apr; 114():79-92. PubMed ID: 16156098
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  • 8. Energy transfer cassettes for facile labeling of sequencing and PCR primers.
    Berti L, Xie J, Medintz IL, Glazer AN, Mathies RA.
    Anal Biochem; 2001 May 15; 292(2):188-97. PubMed ID: 11355850
    [Abstract] [Full Text] [Related]

  • 9. Detection of single base alterations in genomic DNA by solid phase polymerase chain reaction on oligonucleotide microarrays.
    Huber M, Losert D, Hiller R, Harwanegg C, Mueller MW, Schmidt WM.
    Anal Biochem; 2001 Dec 01; 299(1):24-30. PubMed ID: 11726180
    [Abstract] [Full Text] [Related]

  • 10. From gels to chips: "minisequencing" primer extension for analysis of point mutations and single nucleotide polymorphisms.
    Syvänen AC.
    Hum Mutat; 1999 Dec 01; 13(1):1-10. PubMed ID: 9888384
    [Abstract] [Full Text] [Related]

  • 11. High-throughput SNP detection based on PCR amplification on magnetic nanoparticles using dual-color hybridization.
    He N, Li S, Liu H.
    Methods Mol Biol; 2009 Dec 01; 578():393-402. PubMed ID: 19768607
    [Abstract] [Full Text] [Related]

  • 12. Multiplex single nucleotide polymorphisms genotyping using solid-phase single base extension on magnetic nanoparticles.
    Liu H, Li S, Liu L, Tian L, He N.
    Anal Biochem; 2009 Mar 01; 386(1):126-8. PubMed ID: 19100705
    [Abstract] [Full Text] [Related]

  • 13. The method of single-nucleotide variations detection using capillary electrophoresis and molecular beacons.
    Wang J, Wang W, Liu Y, Duo L, Huang L, Jiang X.
    Mol Biol Rep; 2009 Sep 01; 36(7):1903-8. PubMed ID: 18989751
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  • 15. Sensitive and simultaneous analysis of five transgenic maizes using multiplex polymerase chain reaction, capillary gel electrophoresis, and laser-induced fluorescence.
    García-Cañas V, González R, Cifuentes A.
    Electrophoresis; 2004 Jul 01; 25(14):2219-26. PubMed ID: 15274006
    [Abstract] [Full Text] [Related]

  • 16. Integrated sample cleanup-capillary electrophoresis microchip for high-performance short tandem repeat genetic analysis.
    Yeung SH, Liu P, Del Bueno N, Greenspoon SA, Mathies RA.
    Anal Chem; 2009 Jan 01; 81(1):210-7. PubMed ID: 19061366
    [Abstract] [Full Text] [Related]

  • 17. Multiplex PCR and minisequencing of SNPs--a model with 35 Y chromosome SNPs.
    Sanchez JJ, Børsting C, Hallenberg C, Buchard A, Hernandez A, Morling N.
    Forensic Sci Int; 2003 Oct 14; 137(1):74-84. PubMed ID: 14550618
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  • 19. SNaPshot® minisequencing analysis of multiple ancestry-informative Y-SNPs using capillary electrophoresis.
    Geppert M, Roewer L.
    Methods Mol Biol; 2012 Oct 14; 830():127-40. PubMed ID: 22139657
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